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2020 - Clinical Data Management (CDM)



VenueSan Francisco, CA, USA - United States USA - United States

KeywordsClinical data management; FDA E6 GCP Guidelines; NIH Policy (SOP 15


Topics/Call fo Papers

Regulatory guidelines for Clinical Data Management
Best practices for data collection
Responsibilities of personnel
Case report form criteria
Maintaining confidentiality of data
Data storage and transferability
Data preparation and quality assurance for accuracy
Data monitoring plan criteria
Data systems validation
Adverse event reporting and coding criteria
What to expect on a monitoring visit
Troubleshooting and resolution of deviations from plan

Last modified: 2020-01-14 03:28:59